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[DOI] [PMC free article] [PubMed] [Google Scholar] 38.Mojarrab S., Bahrami F., Khoshbaten A., Shojaei A., Daftarian N., Salem F., et al

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July 20: Four years after it was rejected by the FDA due to safety concerns, Daiichi Sankyos Vanflyta (quizartinib) won approval to treat patients with acute myeloid leukemia that has a FLT3-ITD gene mutation

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Methods 14 , 417419 (2017)

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Giuliano F (2006)

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